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GB2086895B - Process for preparation of substituted benzyl phenylacetates - Google Patents

Process for preparation of substituted benzyl phenylacetates

Info

Publication number
GB2086895B
GB2086895B GB8132619A GB8132619A GB2086895B GB 2086895 B GB2086895 B GB 2086895B GB 8132619 A GB8132619 A GB 8132619A GB 8132619 A GB8132619 A GB 8132619A GB 2086895 B GB2086895 B GB 2086895B
Authority
GB
United Kingdom
Prior art keywords
sub
sup
alkyl
formula
benzyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB8132619A
Other versions
GB2086895A (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eli Lilly and Co filed Critical Eli Lilly and Co
Publication of GB2086895A publication Critical patent/GB2086895A/en
Application granted granted Critical
Publication of GB2086895B publication Critical patent/GB2086895B/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D505/00—Heterocyclic compounds containing 5-oxa-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. oxacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D309/10—Oxygen atoms
    • C07D309/12—Oxygen atoms only hydrogen atoms and one oxygen atom directly attached to ring carbon atoms, e.g. tetrahydropyranyl ethers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

A process for preparing a benzyl phenyl-acetate of the formula Iwherein R<sup>1</sup> is hydroxy, protected hydroxy, hydrogen, C<sub>1</sub>-C<sub>4</sub> alkyl, C<sub>1</sub>-C<sub>4</sub> alkoxy or halo; one of R<sup>2</sup> and R<sup>3</sup> is hydrogen and the other is phenoxy or C<sub>1</sub>-C<sub>6</sub> alkoxy; which comprises reacting an alkali metal phenylacetate of the formula IIwith a benzyl halide of the formula IIIwherein M is sodium or potassium, and X is chloro or bromo; in an organic solvent which is inert to esterification and in which the phenylacetic acid salt is substantially insoluble. and in the presence of a catalytic amount of a phase transfer catalyst of. the formulawherein X' is chloro, bromo, iodo, toluenesulfonate or methanesulfonate; R<sup>4</sup> and R<sup>5</sup> are independently C<sub>1</sub>-C<sub>16</sub> alkyl, phenyl or benzyl: R<sup>6</sup> and R<sup>7</sup> are independently C<sub>1</sub>-C<sub>16</sub> alkyl; provided that. when X<sup>1</sup> is a group other than iodo, the process is carried out in the presence of from 0.1 to 0.5 mole of an alkali metal iodide per mole of product to be produced.
GB8132619A 1980-11-03 1981-10-29 Process for preparation of substituted benzyl phenylacetates Expired GB2086895B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/203,736 US4334079A (en) 1980-11-03 1980-11-03 Synthesis of substituted benzyl esters

Publications (2)

Publication Number Publication Date
GB2086895A GB2086895A (en) 1982-05-19
GB2086895B true GB2086895B (en) 1985-09-11

Family

ID=22755118

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8132619A Expired GB2086895B (en) 1980-11-03 1981-10-29 Process for preparation of substituted benzyl phenylacetates

Country Status (9)

Country Link
US (1) US4334079A (en)
EP (1) EP0051457B1 (en)
JP (1) JPS57106643A (en)
AT (1) ATE17113T1 (en)
DE (1) DE3173330D1 (en)
DK (1) DK482681A (en)
ES (1) ES8206431A1 (en)
GB (1) GB2086895B (en)
IE (1) IE52059B1 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3225290A1 (en) * 1982-07-07 1984-01-12 Merck Patent Gmbh RING CONNECTIONS
JP2556026B2 (en) * 1986-04-03 1996-11-20 日産化学工業株式会社 A useful carboxylic acid recovery method from alkaline wastewater
US5084270A (en) * 1988-04-22 1992-01-28 Revlon, Inc. Cosmetic compositions containing N-alkoxyalkylamides
FR2681595B1 (en) * 1991-09-24 1994-09-02 Rhone Poulenc Chimie PROCESS FOR THE ESTERIFICATION OF SALTS OF CARBOXYLIC ACIDS.
US9365486B2 (en) * 2014-07-01 2016-06-14 Muhammed Majeed Synthesis of calebin-A and its biologically active analogs
KR102115644B1 (en) * 2017-09-13 2020-05-27 주식회사 동도물산 Method of manufacturing 7α-alkoxy oxacephem intermediate compound
CN112480147A (en) * 2019-09-12 2021-03-12 杭州森泽医药科技有限公司 Latamoxef intermediate solvate and preparation method and characterization thereof
CN110885287B (en) * 2019-12-04 2022-06-10 安徽圣诺贝化学科技有限公司 Synthetic method for synthesizing isooctyl salicylate from sodium salicylate

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3035084A (en) * 1960-10-04 1962-05-15 Reaction rates of methallyl chloride with
US3651050A (en) * 1969-01-23 1972-03-21 Pfizer Acylation of 6-aminopenicillanic acid and 7-aminocephalosporanic acid
GB1426557A (en) * 1972-10-05 1976-03-03 Beecham Group Ltd Production of substituted monomalonate esters and their use in the production of alpha-carboxy penicillins and cephalosporins
DE2330838A1 (en) * 1973-06-16 1975-01-09 Thomae Gmbh Dr K NEW CARBONIC ACID ESTERS OF 3- (4-BIPHENYLYL) -1-BUTANOLS AND 3- (4-BIPHENYLYL) 2-BUTEN-1-OLEN
JPS5228790B2 (en) * 1973-08-28 1977-07-28
GB1559799A (en) * 1975-11-12 1980-01-30 Shell Int Research Process for preparing substituted benzylesters
DE2622456A1 (en) * 1976-05-20 1977-12-01 Bayer Ag METHOD FOR PRODUCING ALPHA-CARBOXYBENZYLPENICILLIN
DE2739854A1 (en) * 1977-09-03 1979-03-15 Bayer Ag FLUORINE-SUBSTITUTED PHENOXYBENZYLOXYCARBONYL DERIVATIVES, METHODS FOR THE PRODUCTION THEREOF AND THEIR USE AS INSECTICIDES AND ACARICIDES

Also Published As

Publication number Publication date
DE3173330D1 (en) 1986-02-06
EP0051457A3 (en) 1982-09-15
US4334079A (en) 1982-06-08
IE812539L (en) 1982-05-03
IE52059B1 (en) 1987-05-27
ES506788A0 (en) 1982-08-16
ATE17113T1 (en) 1986-01-15
EP0051457B1 (en) 1985-12-27
ES8206431A1 (en) 1982-08-16
JPS57106643A (en) 1982-07-02
GB2086895A (en) 1982-05-19
EP0051457A2 (en) 1982-05-12
DK482681A (en) 1982-05-04

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Legal Events

Date Code Title Description
7732 Case decided by the comptroller ** patent revoked (sect. 73(2)/1977)